logo
Home  > (R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene

AI56086

76189-55-4 | (R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene

Packsize Purity Availability Price Discounted Price    Quantity
1g 99% (99.5%ee) in stock $9.00 $6.00 -   +
5g 99% (99.5%ee) in stock $19.00 $14.00 -   +
25g 99% (99.5%ee) in stock $61.00 $43.00 -   +
500g 99% (99.5%ee) in stock $1,184.00 $829.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AI56086
Chemical Name: (R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene
CAS Number: 76189-55-4
Molecular Formula: C44H33P2
Molecular Weight: 623.6803
MDL Number: MFCD00010805
SMILES: c1ccc(cc1)P(C1=CC=c2c(=[CH]1c1c(ccc3c1cccc3)P(c1ccccc1)c1ccccc1)cccc2)c1ccccc1

 

Upstream Synthesis Route
  • In chemical synthesis, (R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl, commonly referred to as BINAPO, serves as a highly valuable chiral ligand. Its intricate structure and specific stereochemistry make it a crucial component in asymmetric catalysis reactions, where it plays a pivotal role in controlling the stereochemistry of the products formed. By acting as a chiral auxiliary, (R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl facilitates the formation of enantiomerically pure compounds, a critical aspect in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its effectiveness in catalyzing various transformations, such as asymmetric hydrogenation and allylic substitution, underscores its significance in modern organic synthesis. The ability of BINAPO to impart chirality and enhance selectivity makes it a go-to ligand for chemists striving to access optically pure molecules with high efficiency and precision.
FEATURED PRODUCTS